SHFM3P1

Split hand/foot malformation (ectrodactyly) type 3 pseudogene 1, also known as SHFM3P1, is a human gene.^[3]

FBXW4P1
Identifiers
Aliases	FBXW4P1, FBW3, FBXW3, SHFM3P1, F-box and WD repeat domain containing 4 pseudogene 1
External IDs	GeneCards: FBXW4P1; OMA:FBXW4P1 - orthologs
Gene location (Human) Chr. Chromosome 22 (human)[1] Band 22q11.23 Start 23,262,767 bp[1] End 23,265,005 bp[1]
Orthologs Species Human Mouse Entrez 26226 n/a Ensembl ENSG00000230701 n/a UniProt n a n/a RefSeq (mRNA) NM_012165 n/a RefSeq (protein) n/a n/a Location (UCSC) Chr 22: 23.26 – 23.27 Mb n/a PubMed search [2] n/a
Wikidata
View/Edit Human